Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Real Time RT-PCR02:57

Real Time RT-PCR

56.7K
Real-time reverse transcription-polymerase chain reaction, or Real-time RT-PCR, is an analytical tool used to determine the expression level of target genes. The method involves converting mRNA to complementary DNA with the help of an enzyme known as reverse transcriptase, followed by the PCR amplification of the cDNA. These two processes can be performed simultaneously in a single tube or separately as a two-step reaction.
The real-time quantification of the number of amplified products is...
56.7K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Joint assessment of white blood cell-to-HDL cholesterol ratio and waist-to-height-hemoglobin A1c for cardiometabolic multimorbidity risk: a prospective cohort study and cross-sectional study.

Frontiers in nutrition·2026
Same author

Ocular IL-1α/IFN-γ Delay the Corneal Wound Healing in Rheumatoid Arthritis Through Mitochondrial Dysfunction and NLRP3 Inflammasome Activation.

Investigative ophthalmology & visual science·2026
Same author

Hybrid vehicle state estimation using closed-form liquid neural networks and nonlinear Kalman filtering.

ISA transactions·2026
Same author

The Riemann Hypothesis manifested in dynamical quantum phase transitions.

Nature communications·2026
Same author

A Camera-Based Multimodal Defect Sensing Framework for Substation Equipment Monitoring via Cross-Modal Feature Mapping.

Sensors (Basel, Switzerland)·2026
Same author

Multiparticle entanglement of nuclear spins in silicon.

Nature communications·2026

Related Experiment Video

Updated: May 24, 2025

Simple Bulk Readout of Digital Nucleic Acid Quantification Assays
06:55

Simple Bulk Readout of Digital Nucleic Acid Quantification Assays

Published on: September 24, 2015

8.2K

Isotope Dilution DNA Logic Circuits for Multiple Output and Absolute Quantification.

Yiyan Zhu1, Chao Wei2, Ziyan Li3

  • 1Key Laboratory of Green Chemistry & Technology, College of Chemistry, Sichuan University, Chengdu 610064, P.R. China.

Analytical Chemistry
|March 6, 2025
PubMed
Summary

This study introduces DNA logic circuits using lanthanide isotopes for precise microRNA quantification. This novel approach overcomes limitations of optical methods, enhancing accuracy for potential cancer biomarker diagnostics.

More Related Videos

Efficient Chromatin Immunoprecipitation using Limiting Amounts of Biomass
14:29

Efficient Chromatin Immunoprecipitation using Limiting Amounts of Biomass

Published on: May 1, 2013

14.2K
DNA Stable-Isotope Probing DNA-SIP
14:57

DNA Stable-Isotope Probing DNA-SIP

Published on: August 2, 2010

44.0K

Related Experiment Videos

Last Updated: May 24, 2025

Simple Bulk Readout of Digital Nucleic Acid Quantification Assays
06:55

Simple Bulk Readout of Digital Nucleic Acid Quantification Assays

Published on: September 24, 2015

8.2K
Efficient Chromatin Immunoprecipitation using Limiting Amounts of Biomass
14:29

Efficient Chromatin Immunoprecipitation using Limiting Amounts of Biomass

Published on: May 1, 2013

14.2K
DNA Stable-Isotope Probing DNA-SIP
14:57

DNA Stable-Isotope Probing DNA-SIP

Published on: August 2, 2010

44.0K

Area of Science:

  • Biotechnology
  • Molecular Diagnostics
  • Nanotechnology

Background:

  • DNA logic circuits offer scalable and accurate computation but face challenges.
  • Optical probes used in DNA circuits suffer from spectral interference for complex analyses.
  • Absolute quantification of analytes in DNA circuits is difficult, hindering interlaboratory comparisons.

Purpose of the Study:

  • To develop a novel DNA logic circuit system for accurate microRNA quantification.
  • To overcome the limitations of spectral interference and absolute quantification in DNA-based computation.
  • To explore the potential of isotopic DNA logic circuits for cancer biomarker diagnosis.

Main Methods:

  • Constructed DNA logic circuits encoded with specific lanthanide isotopes (gadolinium-155 and neodymium-145).
  • Utilized isotope dilution coupled with elemental mass spectrometry for signal decoding and quantification.
  • Incorporated enriched 155Gd and 145Nd isotopes for precise microRNA detection.

Main Results:

  • The developed isotopic DNA logic circuits demonstrated enhanced multiplexity and computational accuracy.
  • Achieved absolute quantification of microRNAs traceable to the international system of units.
  • Successfully addressed spectral overlapping interference issues inherent in optical detection methods.

Conclusions:

  • Isotopic DNA logic circuits offer a robust platform for sensitive and accurate microRNA detection.
  • This technology significantly improves the reliability of DNA logic circuit-based diagnostics.
  • The approach holds great potential for advancing cancer biomarker discovery and clinical diagnosis.